Llwytho...
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing
The detection of copy number variations (CNVs) on whole-exome sequencing (WES) represents a cost-effective technique for the study of genetic variants. This approach, however, has encountered an obstacle with high false-positive rates due to biases from exome sequencing capture kits and GC contents....
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Evol Bioinform Online |
|---|---|
| Prif Awduron: | , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
SAGE Publications
2020
|
| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7520931/ https://ncbi.nlm.nih.gov/pubmed/33029071 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1176934320956577 |
| Tagiau: |
Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
|